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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2291290생성일: 2026년 10월 25일

Ethanol → Ethyl 5-amino-1-cyclopropyl-6,8-difluoro-7-(3-methyl-1-piperazinyl)-1,4-dihydro-4-oxoquinoline-3-carboxylate

https://huagongshe.com/reaction/2291290

반응식

참여 물질

역할이름HCID투입량
반응물EthanolHCID 702—
반응물Sulfuric AcidHCID 1118—
반응물3-Quinolinecarboxylic acid, 1,4-dihydro-5-amino-1-cyclopropyl-6,8-difluoro-7-(3-methyl-1-piperazinyl)-4-oxo-HCID 3066684—
생성물Ethyl 5-amino-1-cyclopropyl-6,8-difluoro-7-(3-methyl-1-piperazinyl)-1,4-dihydro-4-oxoquinoline-3-carboxylateHCID 14370076—

반응 단계

5-Amino-1-cyclopropyl-6,8-difluoro-7-(3-methyl-1-piperazinyl)-1,4-dihydro-4-oxoquinoline-3-carboxylic acid was suspended in absolute ethanol. Concentrated sulfuric acid was added to the suspension and the mixture was refluxed for 10 hours with stirring. After evaporation of ethanol, chloroform and a 20% aqueous sodium hydroxide solution were added to the residue, and the mixture was adjusted to pH 9. The organic layer was separated and chloroform was evaporated under reduced pressure. The resulting crystals were collected by filtration to give ethyl 5-amino-1-cyclopropyl-6,8-difluoro-7-(3-methyl-1-piperazinyl)-1,4-dihydro-4-oxoquinoline-3-carboxylate, m.p. 132°-134° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04795751
출처 데이터셋uspto-grants-1989_01
ORD IDord-236a385219664cfd8865c39d41ff502b
출처 메모uspto-grants-1989_01